Medline Industries, LP: Device Recall

Recall #Z-0471-2026 · 10/01/2025

Class II: Risk

Recall Details

Recall Number
Z-0471-2026
Classification
Class II
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
10/01/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2 units

Reason for Recall

Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.

Product Description

Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Distribution Pattern

US Nationwide distribution.

Other Recalls by Medline Industries, LP

View all recalls by Medline Industries, LP →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.